K-number	K080101
Device name	AAP CANNULATED SCREW AND DARCO HEADED SCREW
Applicant	Aap Implantate AG
Product code	HWC
Device class	Class II
Decision date	Mar 25, 2008
Decision	Substantially Equivalent
Regulation	888.3040

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View the full FDA submission: accessdata.fda.gov

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AAP CANNULATED SCREW AND DARCO HEADED SCREW

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